FDA UDI In Commercial Distribution 🇺🇸 United States

CUVUR

DI: 00850044290086 · Model: LARGE · Cuvur LLC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
CUVUR
Primary DI
00850044290086
Version / Model
LARGE
Catalog Number
N/A
Company Name
Cuvur LLC
Labeler DUNS
082603210
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2023-03-14
Public Version
1
Public Version Date
2023-03-22
Public Version Status
New
Public Device Record Key
183bb57d-e7e8-483b-af86-95d0e25cd97c

Device Description

NITRILE EXAMINATION GLOVES

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LZA Polymer Patient Examination Glove

GMDN Terms

Code Name
56286 Nitrile examination/treatment glove, non-powdered, non-antimicrobial

Identifiers

Type ID
Package 20850044290035
Primary 00850044290086
Unit of Use 00850044290031

Customer Contacts

Phone
9172317478